Canonical Allele Identifier: CA1619249701
Gene: APOM HGNC NCBI
BAG6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31654914A= , CM000668.2:g.31654914A= GRCh38
NC_000006.11:g.31622691A= , CM000668.1:g.31622691A= GRCh37
NC_000006.10:g.31730670A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000375918.6:c.-102-1558A= (APOM) ENSP00000365083.2:n.-102-1558A=
ENST00000375920.8:c.-102-1558A= (APOM) ENSP00000365085.4:n.-102-1558A=
NM_001256169.1:c.-102-1558A= (APOM) NP_001243098.1:n.-102-1558A=
NR_045828.1:n.143-1558A= (APOM)
XM_011514895.1:c.-13-3138T= (BAG6) XP_011513197.1:n.-13-3138T=
XM_017011279.2:c.-13-3138T= (BAG6) XP_016866768.1:n.-13-3138T=
XM_024446545.1:c.-14+2850T= (BAG6) XP_024302313.1:n.-14+2850T=
NM_001256169.2:c.-102-1558A= (APOM) NP_001243098.1:n.-102-1558A=
NR_045828.2:n.149-1558A= (APOM)
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